Thuy supports the operational delivery of in-trial patient interview studies at CLINIGMA®, contributing to the planning, coordination, and documentation required for successful execution of global clinical projects. With a background in administrative coordination and qualitative research support, she ensures that cross-functional trial activities are tracked accurately and completed on time. Thuy holds a Bachelor’s degree in Human Development and is trained in Good Clinical and Documentation Practices (GCP/GDocP), bringing both regulatory awareness and a strong patient-centred ethic to her work.

Clinical and Research Coordination

• Experience supporting large-scale clinical research initiatives including qualitative studies focused on caregiver interviews
• Skilled in coordinating logistics for remote interviews and document workflows across multiple stakeholder teams
• Trained in Good Clinical Practice (GCP) and Good Documentation Practice (GDocP) for compliance in trial documentation

Operational Support and Project Execution

• Provides administrative and operational support across CLINIGMA® studies, from interview scheduling to data management
• Maintains organized, traceable records of project activities to support data integrity and quality control

Communication and Team Collaboration

• Proven ability to collaborate effectively with internal research teams, clinical partners, and sponsors
• Brings a strong service ethic and people-first approach to day-to-day responsibilities
• Experienced in navigating fast-paced trial environments while balancing multiple administrative priorities

Thuy’s proactive coordination and commitment to quality help ensure the smooth delivery of interview-based studies at CLINIGMA®. Her dual focus on people and process makes her a valued contributor to trial operations.